eudamed_udi Primary ID: 03322541078919

RIVIERA BRONZE T40 (UDI 03322541078919)

Manufactured by GIBAUD

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The RIVIERA BRONZE T40 (Model/Catalog Number: 8434-40) is a medical device manufactured by GIBAUD. This product is indexed under FDA Product Code / Category Classification Y063303 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 8434-40
Product Code / EMDN: Y063303
Device Name: VENISE noir T35
Database Sync Date: 2026-08-09 16:29:18

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of RIVIERA BRONZE T40?

The registered manufacturer of record for RIVIERA BRONZE T40 is GIBAUD.

What is the Primary UDI-DI identifier for RIVIERA BRONZE T40?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03322541078919.

What classification code is assigned to this device?

This device is registered under product classification code Y063303.

Similar Classification Devices (Y063303)

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